A Fetus with Hypertrophic Cardiomyopathy, Restrictive, and Single-Ventricle Physiology, and a β-Myosin Heavy Chain Mutation-Reference-Cited by-同舟云学术

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A Fetus with Hypertrophic Cardiomyopathy, Restrictive, and Single-Ventricle Physiology, and a β-Myosin Heavy Chain Mutation

Published:2010-07 Issue:1 Volume:157 Page:164-166
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Hinton Robert B.,Michelfelder Erik C.,Marino Bradley S.,Bove Kevin E.,Ware Stephanie M.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference4 articles.

1. A contemporary approach to hypertrophic cardiomyopathy;Ho;Circulation,2006

2. Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype;Kubo;J Am Coll Cardiol,2007

3. Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain;Ware;Clin Genet,2008

4. Hypertrophic cardiomyopathy in infants: clinical features and natural history;Maron;Circulation,1982

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. New Genetic Variant in the MYH7 Gene Associated With Hypoplastic Right Heart Syndrome and Hypertrophic Cardiomyopathy in the Same Family;Circulation: Genomic and Precision Medicine;2023-12

2. MYH7 variants cause complex congenital heart disease;American Journal of Medical Genetics Part A;2022-05-02

3. Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling;Reviews in Cardiovascular Medicine;2022-03-17

4. Fetal Cardiovascular Disease;Pathology of Heart Disease in the Fetus, Infant and Child;2019-08-31

5. A Restrictive Cardiomyopathy Mutation in an Invariant Proline at the Myosin Head/Rod Junction Enhances Head Flexibility and Function, Yielding Muscle Defects in Drosophila;Journal of Molecular Biology;2016-06

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